Tc. Randall et al., GERMLINE MUTATIONS OF THE BRCA1 AND BRCA2 GENES IN A BREAST AND OVARIAN-CANCER PATIENT, Gynecologic oncology (Print), 70(3), 1998, pp. 432-434
A patient with breast carcinoma diagnosed at the age of 30 years and o
varian carcinoma diagnosed at the age of 41 years was found to have ge
rmline mutations in both the BRCA1 and the BRCA2 genes. The patient wa
s of Ashkenazi Jewish descent and the BRCA2 mutation was 6174delT, kno
wn to be very common in this population. The BRCA1 mutation, however,
was 3888delGA, a mutation not previously reported in this ethnic group
. The patient's breast cancer exhibited loss of heterozygosity (LOH) a
t the BRCA1 locus but not at BRCA2, and her ovarian cancer sustained L
OH at BRCA1 and BRCA2, The BRCA1 mutation originated from patient's fa
ther, who had no personal or family history of cancer. The patient's m
other, who was found to carry the BRCA2 mutation, was affected by late
-onset breast cancer and her tumor exhibited LOH at BRCA2, These findi
ngs indicate that compound heterozygotes for germline mutations of BRC
A1 and BRCA2 exist and may be expected to develop normally and that ei
ther gene may contribute to breast or ovarian cancer development in su
ch individuals. The implications of this case in regard to genetic tes
ting and counseling are also substantial, (C) 1998 Academic Press.